{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
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      "state": "MN",
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      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Microbiologics Inc",
      "address_1": "200 Cooper Ave N",
      "address_2": "",
      "postal_code": "56303-4440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
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      "product_description": "Inactivated macrolide and quinolone-resistant Mycoplasma genitalium",
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      "termination_date": "20230109",
      "report_date": "20220427",
      "code_info": "Catalog HE0069N; Lot HE0069-02-1 UDI: 10845357043990",
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}